Choosing Moxie


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The beginning of my pregnancy with Moxie feels jumbled, as I recollect it now, some 3 years later. It’s a blur of happenings, events moving swiftly upon each other like quick waves that peak in a tsunami. The blur may be due to the events themselves or may be to the way my mind works – I have brain injury, sustained from jetting out of the windshield of a car when I was four. Memories for me often shape themselves in unusual ways.

Like the day that we went to see our daughter for the first time.

I remember being in a black short dress with pirate sleeves that was from H&M, with black flared yoga pants. I liked that dress. I remember wanting to wear cherry red lipstick and not having any. I remember I wore my Earth moonboots and that Mikey didn’t like them. I remember that we passed a moss green Nissan Cube on the way there. I remember the weather was crisp, dry and clear. I think I was about 10 weeks pregnant. I know I was 36 years old (I just did the math). I also know that I was pregnant after just having had a second trimester miscarriage.

We were on our way to the special clinic, the one where they send “higher risk” pregnancies to be examined. Once there, in the dim room with the brightness of the ultrasound machine in front of us, my belly exposed with glistening gel slathered on, we saw the blinking of our baby’s heart, knew she was alive and for that, were happy. But we knew that the long pause and the lack of chatter from the technician signaled a problem. She left, and returned with the very same perinatologist who had told me that my last child had died. My heart sank as I saw him and I blurted out something along the lines of, “but the baby is alive! I know it! I can see the heart beating!”

He nodded. Yes, our baby was alive but there were problems. He showed us the line of her skin and the line of her body: they were clearly separated. She had a condition called diffuse fetal hydrops, in which her skin was completely separated from her body, with fluid lying between the two. She had heart holes. She was unlikely to make it to term. “0%” chance of survival, he gave her.  He suggested that we have an amniocentesis before she died to find out the cause of the hydrops – not necessarily for her as she was clearly beyond saving – but for future pregnancies.

Numb, and with aching hearts, we consented and returned a few weeks later for the test.

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The amniocentesis revealed the presence of an extra chromosome. It also revealed that the baby was a girl. And miraculously – her diffuse fetal hydrops had completely resolved itself.

Despite being strongly encouraged to terminate her life on account of the Down syndrome, we chose to keep her. Perhaps I should be more honest here: my husband chose to keep her. My husband was adamant about keeping her, saying that we needed to “play with the cards we are given.”

Continuing in this vein of honesty, I am not sure I would have kept her, had I not been with him.

Having grown up deaf, with brain injury and with my auditory processing disorder – not to mention with scars all over my face, I know what it’s like to grow up with a disability. I know what it’s like to be excluded, mocked, and outcast. I know what it’s like to literally have stones thrown at you, because you are different, an “other”. I have a chip in my front tooth from a time that I fought back, but the (much larger) boy was wearing a ring when he punched me in the mouth.

I have been abused. I have been raped. And I am the norm in this: statistics clearly show that up to 90% of people with disabilities have been sexually abused, a disproportionate number of those being people with intellectual disabilities.

Why then would I consciously choose to bring a daughter into this world, knowing full well that I could be exposing her to what I have been exposed to? Why would I choose to open the doors to the potential for boundless suffering? Keeping her seemed to be an act of pure selfishness.

Selfish, you see, because I did want her. I wanted her with all of my heart.



I deeply regretted having the amniocentesis. I regretted knowing that she’d be coming with Down syndrome. My angst over our decision to keep her consumed me, kept me awake for most of my pregnancy, endless insomnia. Night after night I’d relive my own most horrific memories, wondering if I made the right choice, if I had simply conscripted my daughter to a life of misery.

Scared, too of Down syndrome and of intellectual disability, I pored over personal blogs, memoirs, articles – anything and everything to ease my fear of that unknown.

I envied people that had a birth diagnosis because I felt that at least they could hold their baby as they wept or dealt with grief. Me? I had to wrap my arms around my moving belly and walk alone amongst the dark thoughts in my own head.

Walking among all the dark thoughts in my head served its purpose though. I finally realized that my daughter’s life is her own and not mine. Her path is fresh and clear and her disability is not mine. The way the world sees her and the way in which she will move and grow will be different from me. As Gibran says,

Your children are not your children.
They are the sons and daughters of Life’s longing for itself.
They come through you but not from you,
And though they are with you yet they belong not to you.

The grief that enveloped me for so much of my pregnancy also served a purpose: it purged me of anything other than my thorough joy and delight in her existence.


Moxie Eleanor.

Light of our lives.


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  1. 3

    Rachel Hillestad says

    Agh! Seriously. Seriously. SERIOUUUUUUUUUUUUUUUSLY.

    This is so gloriously beautiful. We were faced with similar choices with our firstborn and I feel like I was living some of those lines.

    This is so beautiful, and you’re a GREAT baby namer!

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  2. 5

    Shell says

    Such a brave and honest post. Thank you for sharing how you really felt. Not every thought we have as a parent is one of sweetness and light- be we can work through it.

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  3. 6

    Sonja Onderko says

    I agree so raw and well written! I have always said children are on loan to us from God, not ours to keep, they have their own path that they must forge. I am so sorry for all the pain in your life but you are a beautiful person … maybe not the path that you would have wanted but a path just as important and full of LOVE!

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  4. 16

    cc fisher says

    I love this! We are a family that adopted a child with Down Syndrome. A little girl. Her parents made the same remarks you did, but they made a very different choice. Husband gets angry with that. I feel nothing but blessed. Because of their choice, we have our daughter. Like your Moxie, our M is equally a blessing to us. Know you are not alone in your feelings. Your husband sounds amazing, calm and steadfast. Got one of those myself. Blessed there, too. BTW: Love the name Moxie. I am sure it will serve your beautiful little girl well. Hugs!

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  5. 17

    Lauren says

    Wow. Just need to say a quick thank you…my son was born with a birth defect and I’ve always been angry that it wasn’t discovered while I was pregnant. Your words about not being able to hold your little one just gave me the slap in the face I needed. Definitely feeling some appreciation….

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